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"68382-072-05" National Drug Code (NDC)
Pravastatin Sodium 500 TABLET in 1 BOTTLE (68382-072-05)
(Zydus Pharmaceuticals USA Inc.)
NDC Code
68382-072-05
Package Description
500 TABLET in 1 BOTTLE (68382-072-05)
Product NDC
68382-072
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Pravastatin Sodium
Non-Proprietary Name
Pravastatin Sodium
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20100330
Marketing Category Name
ANDA
Application Number
ANDA077751
Manufacturer
Zydus Pharmaceuticals USA Inc.
Substance Name
PRAVASTATIN SODIUM
Strength
40
Strength Unit
mg/1
Pharmacy Classes
HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68382-072-05